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2-diethoxyphosphanyloxy-[1,3,2]dioxaphospholane | 829-89-0

中文名称
——
中文别名
——
英文名称
2-diethoxyphosphanyloxy-[1,3,2]dioxaphospholane
英文别名
O-[1,3,2]dioxaphospholan-2-yl-phosphorous acid diethyl ester;diphosphorus (III)-oic acid-1,1-ethanediyl ester-2,2-diethyl ester;Diphosphor(III)-saeure-1,1-aethandiylester-2,2-diaethylester;Diphosphorigsaeure-1,1-aethandiylester-2,2-diaethylester;1,3,2-Dioxaphospholan-2-yl diethyl phosphite
2-diethoxyphosphanyloxy-[1,3,2]dioxaphospholane化学式
CAS
829-89-0
化学式
C6H14O5P2
mdl
——
分子量
228.122
InChiKey
AOEOETNVZQDCJK-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    0.6
  • 重原子数:
    13
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    46.2
  • 氢给体数:
    0
  • 氢受体数:
    5

SDS

SDS:081da8819ab796dba9b500d66cce85bf
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反应信息

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文献信息

  • t-Butyloxycarbonylamino Acids and Their Use in Peptide Synthesis
    作者:George W. Anderson、Anne C. McGregor
    DOI:10.1021/ja01580a020
    日期:1957.12
  • Mechanism of the reactions of trialkyl phosphites with ?-halocarbonyl compounds
    作者:T. Kh. Gazizov、A. M. Pyndyk、Yu. I. Sudarev、V. B. Podobedov、V. I. Kovalenko、A. N. Pudovik
    DOI:10.1007/bf00946685
    日期:1978.11
  • Catalyst Composition with Phosphorus-Based Donor and Method
    申请人:Coalter, III Joseph N.
    公开号:US20100227988A1
    公开(公告)日:2010-09-09
    Disclosed are catalyst compositions having an external electron donor which includes one or more of the following compositions: a phosphite, a phosphonite, a pyrophosphite, and/or a diphosphazane. Ziegler-Natta catalyst compositions containing the present external electron donor exhibit strong activity and produce propylene-based olefins with high isotacticity and high melt flow rate.
  • US8614162B2
    申请人:——
    公开号:US8614162B2
    公开(公告)日:2013-12-24
  • [EN] CATALYST COMPOSITION WITH PHOSPHORUS-BASED DONOR AND METHOD<br/>[FR] COMPOSITION DE CATALYSEUR AVEC DONNEUR À BASE DE PHOSPHORE ET PROCÉDÉ CORRESPONDANT
    申请人:DOW GLOBAL TECHNOLOGIES INC
    公开号:WO2010078330A2
    公开(公告)日:2010-07-08
    Disclosed are catalyst compositions having an external electron donor which includes one or more of the following compositions: a phosphite, a phosphonite, a pyrophosphite, and/or a diphosphazane. Ziegler-Natta catalyst compositions containing the present external electron donor exhibit strong activity and produce propylene-based olefins with high isotacticity and high melt flow rate.
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同类化合物

尿苷5'-二磷酸酯溴乙酰醇 N,N-二乙基-4-甲基-1,3,2-二氧杂磷杂环戊烷-2-胺 4,4,5,5-四甲基-1,3,2-二氧磷杂环戊烷-2-醇 2-氯-4-甲基-1,3,2-二氧杂磷杂环戊烷 2-氯-4,4,5,5-四甲基-1,3,2-二氧磷杂环戊烷 2-氯-1,3,2-二氧磷杂环戊烷 (3,5-二甲基苯基)[羟基(吡啶-4-基甲基)-lambda~5~-氮烷基]甲酮 2-Dipropylamino-<1,3,2 λ3>dioxaphospholan 2-ethoxy-[1,3,2]oxazaphospholidine Ethylen-2.2.2-trifluorethylphosphit-ozonid 2-dimethylamino-(3ar,9ac,3'ar',9'ac')-hexadecahydro-2λ5-[2,2']spirobi(cycloocta[1,3,2]dioxaphosphole) 2,7-dimethyl-1,4,6,9-tetraoxa-5(λ5)-phosphaspiro<4.4>nonane Aethylenselenit 4,5-bis-trifluoromethyl-2λ5-spiro[[1,3,2]dioxaphosphole-2,1'-(2,8,9-trioxa-1-phospha-adamantane)] 5,5-Difluoro-1,4,6,9-tetraoxa-5λ6-tellura-spiro[4.4]nonane N-methyl-1-(1,4,6,9-tetraoxa-5λ5-phosphaspiro[4.4]nonan-5-yl)-N-(1,4,6,9-tetraoxa-5λ5-phosphaspiro[4.4]nonan-5-ylmethyl)methanamine 2-methyl-5-(2,2,2-trichloroethoxy)-1,4,6,9-tetraoxa-5λ5-phosphaspiro[4.4]nonan-3-one Butan-2,3-diylselenit (4r,5t-dimethyl-[1,3,2]dioxaphospholan-2-yl)-dimethyl-amine 3,3-dibromo-2-fluoro-4-propyl-1,2λ5-oxaphosphetane 2-Fluor-2,2-dibrom-4,4,5,5-tetrakis-(trifluormethyl)-(1,3,2λ5-dioxaphospholan [1,3,2]dioxaphospholan-2-yl-ethyl-amine 2-tert-butylamino-2,2-difluoro-4,4,5,5-tetrakis-trifluoromethyl-2λ5-[1,3,2]dioxaphospholane 3,3-dichloro-2-fluoro-4-propyl-1,2λ5-oxaphosphetane 1,1-Dibromo-3,5,8-tris-(1,1,2,2-tetrafluoro-ethyl)-2,6,7-trioxa-1λ5,4-diphospha-bicyclo[2.2.2]octane 2-Brom-4,4,5,5-tetrakis-(trifluormethyl)-(1,3,2λ5-dioxaphospholan dibutyl-(4-methyl-[1,3,2]dioxaphospholan-2-yl)-amine 2-(tert-butylimino)-1,3,2,4-oxaazaphosphaboretidine 1,1,3,3,5,5,7,7-Tetrakis--tetraphosphazatetraen 2-Chlor-2,2-dibrom-4,4,5,5-tetrakis-(trifluormethyl)-(1,3,2λ5-dioxaphospholan 2-Propoxy-[1,3,2]dioxaphospholan-4-one 2-Fluor-2,2-dichlor-4,4,5,5-tetrakis-(trifluormethyl)-(1,3,2λ5-dioxaphospholan 2-fluoro-3-methyl-[1,3,2]oxazaphospholidine 2,2,2,4-tetrachloro-3-isopropyl-4-triflyoromethyl-1,3,2-λ5-oxazaphosphetane 1,1-Dichloro-3,5,8-tris-(1,1,2,2-tetrafluoro-ethyl)-2,6,7-trioxa-1λ5,4-diphospha-bicyclo[2.2.2]octane 2-ethoxy-2-fluoro-2λ5-[1,3,2]dioxaphospholan-2-yl phosphoric acid-(2-ethyl-2-butyl-propanediyl ester)-(2-bromo-propyl ester) (4,4-dimethyl-1,3,2-dioxaphospholan-2-yl) 2,2,2-trifluoroacetate 2-Dimethylamino-4,4,5,5-tetrakis(trifluormethyl)-1,3,2λ3-dioxaphospholan 2,3,3-Trichloro-2,2-diethyl-4-trichloromethyl-2λ5-[1,2]oxaphosphetane (5-tert-butyl-[1,3,2]dioxaphosphinan-2-yl)-dimethyl-amine 2-cyclohexyl-[1,3,2]dioxaphospholane (4-tert-Butyl-[1,3,2]dioxaphospholan-2-yl)-diethyl-amine N-Methyl-N-[1-methyl-2-(4,4,5,5-tetramethyl-[1,3,2]dioxaphospholan-2-yloxy)-propyl]-acetamide 2,2-Dichlor-2-dimethylamino-4,4,5,5-tetrakis(trifluormethyl)-1,3,2λ5-dioxaphospholan methyl-2-trioxaphosphocanne-1,3,6,2 5-dimethylamino-2,4-diisopropylidene-1,3,6,9-tetraoxa-5λ5-phospha-spiro[4.4]nonane